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Biomedical subjects

D J Lacey

Publications and source records attributed to D J Lacey.

25 records · Page 2Linked to original sources

Rectal absorption and disposition of secobarbital in epileptic children.

The absorption and disposition of rectally administered secobarbital was studied in ten epileptic children, ages 2-13 yrs. Five subjects received secobarbital rectally in solution, and the other five received secobarbital suppositories. Concentration of secobarbital in serum was serially determined during 48 hrs after a single rectal dose of about 5 mg/kg. The rate of absorption of secobarbital, as measured by the time to reach peak serum concentration, was much more rapid from the solution than the suppository (0.92 +/- 0.47 hr vs 4.60 +/ 2.30 hr). The peak serum concentration of secobarbital in the solution group was consistently higher than in the suppository group (2.26 +/- 0.37 micrograms/ml vs 1.35 +/- 0.24 microgram/ml). None of the individual peak serum concentrations exceeded 3 micrograms/ml, which is well below the previously reported minimum toxic concentration of secobarbital (ie, 6 microgram/ml). The elimination half-life of secobarbital varied over a wide range, from 2.7 to 13.5 hr, and is, on the average, shorter than estimates previously reported for adult volunteers or poly-drug abusers. Also, the mean elimination half-life did not differ between the solution and the suppository groups. The extent of rectal absorption of secobarbital, as assessed by the area under the serum concentration time curve, was not significantly different between the solution and the suppository treatments. If rectal secobarbital is considered for treatment of prolonged seizure, a rectal solution may offer a more rapid and consistent onset of action than with the suppository preparation.

Adolescent↗

Neurologic sequelae of acute carbon monoxide intoxication.

Notable neuropsychologic symptoms persist in a 9-year-old girl one year after an acute exposure to carbon monoxide (CO). Perceptual deficits, personality alterations, and computerized tomographic evidence of leukoencephalopathy persist. Three of five children admitted between 1973 and 1978 with the diagnosis of acute CO intoxication also have residual behavioral and/or school difficulties. Physicians caring for children should consider CO poisoning in the differential diagnosis of an acute encephalopathic state and anticipate its potentially long-term effects.

Brain Diseases↗

The organization of the hippocampus of the fence lizard: a light microscopic study.

The hippocampus of the fence lizard (Sceloporus undulatus) is composed of two laminated regions that are readily distinguishable on the basis of position and perikaryal size in Nissl preparations: the small-celled (Hsc) and the large-celled (Hlc) hippocampal divisions. Based upon cellular and fibrillar characteristics, the layers of the Hsc are: (1) the superficial plexiform layer; (2) the cellular layer; (3) the deep plexiform layer; (4) the layer of deep fibers, or alveus; and, (5) the ventricular ependyma. The layers of the Hlc are: (1) the tangential layer; (2) the molecular layer; (3) the pyramidal layer; (4) the deep plexiform layer; (5) the alveus; and, (6) the ventricular ependyma. The neurons of each hippocampal layer were grouped into classes based upon somal position and appearance, and dentritic and axonal arborization patterns in Golgi sections. Neurons of the Hsc are more numerous and pleomorphic than those of the Hlc. Data do not suggest an intrinsic organization that closely parallels that found in the mammalian hippocampus.

Animals↗

Inability to verify parasagittal cerebral injury as a neuropathologic entity in the asphyxiated term neonate.

Localization of brain injury to parasagittal arterial border zones in the asphyxiated term neonate has been recently described as a frequent, clinically significant finding. However, pathologic examination of the brains of 79 term infants did not reveal a parasagittal distribution of damage. Coronal CT scans of 13 asphyxiated neonates with clinical findings of proximal hypotonia, and repeat scans 6-12 months later in seven patients, have not demonstrated watershed areas of decreased density. A larger series of prospectively identified, surviving neonates is needed to determine whether clinically relevant parasagittal injury may be present in this population.

Asphyxia Neonatorum↗

Unusual biochemical and clinical features in a girl with ornithine transcarbamylase deficiency.

A girl, ultimately diagnosed as having profound ornithine transcarbamylase (OTC) deficiency, presented as a neonate with feeding intolerance, irritability, and seizures without concurrent hyperammonemia. Developing normally until ten months of age, the girl subsequently experienced two episodes of hyperammonemia, which were associated with focal seizures and residual hemiparesis. She continued to have profound neurologic impairment and seizures and died at 26 months of age, despite appropriate dietary protein restriction, sodium benzoate, and arginine supplementation. Symptomatic OTC deficiency has not been previously reported unassociated with hyperammonemia. The recurrent cerebrovascular episodes are distinctly uncommon in patients with urea cycle enzymopathies.

Amino Acid Metabolism, Inborn Errors↗